View genomic variant #0000023467

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19373511A>C
Published as -
GERP -
Segregation -
DB-ID PDHA1_000010 See all 2 reported entries
MSCV MSCV_0001526
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
PDHA1 00000247 NM_000284.3 0000023467 ./. - - c.648A>C p.(Leu216Phe) - - - -
PDHA1 00000245 NM_001173454.1 0000023467 ./. - - c.762A>C p.(Leu254Phe) - - - -
PDHA1 00000246 NM_001173455.1 0000023467 ./. - - c.669A>C p.(Leu223Phe) - - - -
PDHA1 00000248 NM_001173456.1 0000023467 ./. - - c.555A>C p.(Leu185Phe) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011640;
Chromosome X:19373511..19373511
ClinVar Allele ID 25932
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19373511A>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121228|OMIM:300502.0023
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121917898
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None